Variant report

Variant	nsv981507
Chromosome Location	chr7:65878773-65886496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:65878572-65878873	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:65878779-65878989	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr7:65882741-65882983	GM12878	blood:	n/a	n/a
4	BCL3	chr7:65878547-65878997	A549	lung:	n/a	chr7:65878577-65878590
5	BHLHE40	chr7:65878479-65878938	GM12878	blood:	n/a	n/a
6	BRCA1	chr7:65878386-65878951	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr7:65885641-65885925	IMR90	lung:	n/a	chr7:65885775-65885786
8	CEBPB	chr7:65885646-65885952	HepG2	liver:	n/a	chr7:65885775-65885786
9	CEBPB	chr7:65878359-65879038	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:65884246-65884541	K562	blood:	n/a	n/a
11	CEBPB	chr7:65885618-65885836	K562	blood:	n/a	chr7:65885775-65885786
12	CEBPB	chr7:65884243-65884558	K562	blood:	n/a	n/a
13	CEBPB	chr7:65884283-65884523	HepG2	liver:	n/a	n/a
14	CHD2	chr7:65878303-65879090	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr7:65878099-65879124	H1-hESC	embryonic stem cell:	n/a	chr7:65878538-65878551
16	CREB1	chr7:65878175-65879126	GM12878	blood:	n/a	chr7:65878538-65878551
17	CREB1	chr7:65878189-65879017	GM12878	blood:	n/a	chr7:65878538-65878551
18	CREB1	chr7:65878196-65879021	A549	lung:	n/a	chr7:65878538-65878551
19	CREB1	chr7:65878223-65879061	ECC-1	luminal epithelium:	n/a	chr7:65878538-65878551
20	CREB1	chr7:65878110-65878955	ECC-1	luminal epithelium:	n/a	chr7:65878538-65878551
21	CREB1	chr7:65878024-65879192	H1-hESC	embryonic stem cell:	n/a	chr7:65878538-65878551
22	CTCF	chr7:65878677-65879006	GM10266	blood:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831 chr7:65878953-65878971
23	CTCF	chr7:65878301-65879151	H1-hESC	embryonic stem cell:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831 chr7:65878953-65878971
24	CTCF	chr7:65878740-65878890	HEEpiC	esophagus:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
25	CTCF	chr7:65878758-65878821	Medullo	brain:	n/a	chr7:65878786-65878794
26	CTCF	chr7:65878740-65878890	HMF	breast:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
27	CTCF	chr7:65878740-65878890	AG04450	lung:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
28	CTCF	chr7:65878660-65878810	GM12872	blood:	n/a	chr7:65878786-65878794
29	CTCF	chr7:65878644-65879082	MCF-7	breast:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831 chr7:65878953-65878971
30	CTCF	chr7:65878720-65878870	AG04449	skin:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
31	CTCF	chr7:65878772-65878902	Kidney_OC	kidney:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
32	CTCF	chr7:65878820-65878970	GM12869	blood:	n/a	n/a
33	CTCF	chr7:65878720-65878870	HPAF	blood vessel:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
34	CTCF	chr7:65878760-65878910	HRPEpiC	eye:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
35	CTCF	chr7:65878780-65878930	GM12867	blood:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
36	CTCF	chr7:65878700-65878850	AoAF	blood vessel:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
37	CTCF	chr7:65878740-65878890	HEK293	kidney:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
38	CTCF	chr7:65878760-65878910	RPTEC	kidney:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
39	CTCF	chr7:65878740-65878890	GM12872	blood:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
40	CTCF	chr7:65878683-65878930	HUVEC	blood vessel:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
41	CTCF	chr7:65878780-65878930	HFF-Myc	foreskin:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
42	CTCF	chr7:65878800-65878950	GM12875	blood:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878808-65878826 chr7:65878810-65878831
43	CTCF	chr7:65878780-65878930	HCFaa	heart:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
44	CTCF	chr7:65878700-65878850	HPAF	blood vessel:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
45	CTCF	chr7:65878740-65878890	AoAF	blood vessel:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
46	CTCF	chr7:65878720-65878870	HCPEpiC	choroid plexus:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
47	CTCF	chr7:65878820-65878970	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr7:65878720-65878870	HL-60	blood:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831
49	CTCF	chr7:65878671-65879054	MCF-7	breast:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831 chr7:65878953-65878971
50	CTCF	chr7:65878558-65879124	MCF-7	breast:	n/a	chr7:65878811-65878824 chr7:65878809-65878825 chr7:65878786-65878794 chr7:65878808-65878826 chr7:65878810-65878831 chr7:65878953-65878971

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65882633-65882683	SK-N-MC	brain:	n/a
2	chr7:65882633-65882683	SK-N-MC	brain:	n/a
3	chr7:65878734-65878784	ovcar-3	ovarian:	n/a
4	chr7:65878734-65878784	LNCaP	prostate:	n/a
5	chr7:65879115-65879165	K562	blood:	n/a
6	chr7:65879115-65879165	HEEpiC	esophagus:	n/a
7	chr7:65878911-65878961	NH-A	brain:	n/a
8	chr7:65878734-65878784	HUVEC	blood vessel:	n/a
9	chr7:65878734-65878784	GM12891	blood:	n/a
10	chr7:65878976-65879026	HAEpiC	amniotic membrane:	n/a
11	chr7:65878734-65878784	Hela-S3	cervix:	n/a
12	chr7:65878734-65878784	BJ	skin:	n/a
13	chr7:65882633-65882683	AG04450	lung:	fetal
14	chr7:65878734-65878784	SK-N-SH_RA	brain:	n/a
15	chr7:65882633-65882683	GM12891	blood:	n/a
16	chr7:65879115-65879165	HL-60	blood:	n/a
17	chr7:65878911-65878961	HMEC	breast:	n/a
18	chr7:65878976-65879026	ovcar-3	ovarian:	n/a
19	chr7:65878976-65879026	AG09309	skin:	n/a
20	chr7:65879115-65879165	HNPCEpiC	eye:	n/a
21	chr7:65878734-65878784	HCT-116	colon:	n/a
22	chr7:65878976-65879026	RPTEC	kidney:	n/a
23	chr7:65878976-65879026	SKMC	muscle:	n/a
24	chr7:65882633-65882683	LNCaP	prostate:	n/a
25	chr7:65882633-65882683	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:65878976-65879026	U87	brain:	n/a
27	chr7:65879115-65879165	AG04449	skin:	fetal
28	chr7:65878911-65878961	HCT-116	colon:	n/a
29	chr7:65879115-65879165	U87	brain:	n/a
30	chr7:65878976-65879026	AoSMC	blood vessel:	n/a
31	chr7:65878976-65879026	GM06990	blood:	n/a
32	chr7:65878734-65878784	HIPEpiC	eye:	n/a
33	chr7:65879115-65879165	BJ	skin:	n/a
34	chr7:65878976-65879026	GM12892	blood:	n/a
35	chr7:65882633-65882683	BJ	skin:	n/a
36	chr7:65879115-65879165	GM12892	blood:	n/a
37	chr7:65878911-65878961	HRPEpiC	eye:	n/a
38	chr7:65878734-65878784	ECC-1	luminal epithelium:	n/a
39	chr7:65879115-65879165	HRPEpiC	eye:	n/a
40	chr7:65882633-65882683	ovcar-3	ovarian:	n/a
41	chr7:65878911-65878961	HCPEpiC	choroid plexus:	n/a
42	chr7:65878911-65878961	SK-N-MC	brain:	n/a
43	chr7:65878911-65878961	AG09319	gingival:	n/a
44	chr7:65879115-65879165	SKMC	muscle:	n/a
45	chr7:65878976-65879026	LNCaP	prostate:	n/a
46	chr7:65879115-65879165	HEK293	kidney:	embryo
47	chr7:65879115-65879165	AG04450	lung:	fetal
48	chr7:65878976-65879026	AG04449	skin:	fetal
49	chr7:65878976-65879026	Hepatocyte	liver:	n/a
50	chr7:65878976-65879026	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:65850442..65853165-chr7:65885977..65887755,2	K562	blood:
2	chr7:65686273..65688117-chr7:65877962..65880122,2	MCF-7	breast:
3	chr7:65883342..65885177-chr7:65887474..65889695,2	K562	blood:

Variant related genes	Relation type
ENSG00000251451	TF binding region
ENSG00000251451	CpG island
ENSG00000231234	chromatin interactions
ENSG00000169902	chromatin interactions

Extended variants
information (count: 290 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114069280	chr7:65878885-65878886	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs527258611	chr7:65878948-65878949	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs548140866	chr7:65879001-65879002	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571137309	chr7:65879017-65879018	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs539715013	chr7:65879025-65879026	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550351322	chr7:65879059-65879060	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs143987105	chr7:65879087-65879088	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184470142	chr7:65879115-65879116	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs76700367	chr7:65879148-65879149	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs572134672	chr7:65879158-65879159	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs62465373	chr7:65879184-65879185	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs188151651	chr7:65879202-65879203	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs79427543	chr7:65879207-65879208	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs577071842	chr7:65879236-65879237	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545739483	chr7:65879239-65879240	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562745504	chr7:65879320-65879321	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569307650	chr7:65879342-65879343	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576303185	chr7:65879397-65879398	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113666640	chr7:65879422-65879423	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144691336	chr7:65879424-65879425	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538287946	chr7:65879434-65879435	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558330637	chr7:65879478-65879479	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192674616	chr7:65879504-65879505	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547388004	chr7:65879507-65879508	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35342701	chr7:65879533-65879534	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs397811444	chr7:65879534-65879535	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs372090927	chr7:65879535-65879536	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148499631	chr7:65879546-65879547	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533686704	chr7:65879559-65879560	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534876949	chr7:65879625-65879626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184751646	chr7:65879653-65879654	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs570276994	chr7:65879697-65879698	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs117642505	chr7:65879760-65879761	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs189206559	chr7:65879762-65879763	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142876338	chr7:65879763-65879764	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534749289	chr7:65879769-65879770	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558143239	chr7:65879833-65879834	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571544137	chr7:65879870-65879871	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375410814	chr7:65879872-65879873	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575119415	chr7:65879873-65879874	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs11763736	chr7:65879883-65879884	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539769882	chr7:65879903-65879904	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181583294	chr7:65879918-65879919	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs186891927	chr7:65879988-65879989	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553782200	chr7:65880028-65880029	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs62465374	chr7:65880035-65880036	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs151050957	chr7:65880055-65880056	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77749267	chr7:65880061-65880062	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530750931	chr7:65880067-65880068	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572171939	chr7:65880082-65880083	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Glioblastoma	21080181	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65861800-65880800	Weak transcription	Hela-S3	cervix
2	chr7:65874800-65883600	Weak transcription	HepG2	liver
3	chr7:65875200-65884400	Weak transcription	K562	blood
4	chr7:65876200-65888600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:65877000-65888600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:65878000-65878800	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr7:65878000-65879200	Active TSS	Brain Substantia Nigra	brain
8	chr7:65878000-65879400	Active TSS	Brain Angular Gyrus	brain
9	chr7:65878000-65879400	Active TSS	Fetal Kidney	kidney
10	chr7:65878000-65879600	Active TSS	Brain Cingulate Gyrus	brain
11	chr7:65878200-65878800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:65878200-65878800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:65878200-65878800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:65878200-65878800	Active TSS	Brain Hippocampus Middle	brain
15	chr7:65878200-65878800	Active TSS	Duodenum Mucosa	Duodenum
16	chr7:65878200-65878800	Active TSS	Fetal Brain Female	brain
17	chr7:65878200-65878800	Active TSS	HUVEC	blood vessel
18	chr7:65878200-65879000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:65878200-65879000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:65878200-65879000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:65878200-65879000	Active TSS	Brain Anterior Caudate	brain
22	chr7:65878200-65879000	Active TSS	A549	lung
23	chr7:65878200-65879200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr7:65878200-65879200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr7:65878200-65879200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:65878200-65879200	Active TSS	Colonic Mucosa	Colon
27	chr7:65878200-65879200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr7:65878200-65879200	Flanking Active TSS	Fetal Brain Male	brain
29	chr7:65878200-65879200	Flanking Active TSS	Fetal Muscle Leg	muscle
30	chr7:65878200-65879200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr7:65878200-65879200	Flanking Active TSS	Stomach Smooth Muscle	stomach
32	chr7:65878200-65879400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:65878200-65879400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:65878400-65878800	Active TSS	Primary B cells from cord blood	blood
35	chr7:65878400-65878800	Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr7:65878400-65878800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr7:65878400-65878800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr7:65878400-65878800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr7:65878400-65878800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:65878400-65878800	Active TSS	Fetal Heart	heart
41	chr7:65878400-65878800	Active TSS	Rectal Smooth Muscle	rectum
42	chr7:65878400-65878800	Active TSS	GM12878-XiMat	blood
43	chr7:65878400-65879000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:65878400-65879000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr7:65878400-65879000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:65878400-65879000	Flanking Active TSS	Primary B cells from peripheral blood	blood
47	chr7:65878400-65879000	Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr7:65878400-65879000	Active TSS	Colon Smooth Muscle	Colon
49	chr7:65878400-65879000	Flanking Active TSS	Esophagus	oesophagus
50	chr7:65878400-65879000	Flanking Active TSS	Fetal Lung	lung

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